Canonical Allele Identifier: CA1537629909
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1740343279
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32689729C>A , CM000667.2:g.32689729C>A GRCh38
NC_000005.9:g.32689835C>A , CM000667.1:g.32689835C>A GRCh37
NC_000005.8:g.32725592C>A NCBI36
NG_028162.2:g.5654C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509104.5:c.100+543C>A ENSP00000425325.1:n.100+543C>A
XM_011514047.1:c.100+543C>A XP_011512349.1:n.100+543C>A
XM_011514047.2:c.100+543C>A XP_011512349.1:n.100+543C>A
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